A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057428



Internal ID18799959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:37791518..37830174hg38UCSC Ensembl
Innerchr19:38282158..38320814hg19UCSC Ensembl
Innerchr19:42973998..43012654hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3838657
hg1938657
hg1838657
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3568192, nssv3568193
Samples
Known GenesLOC100631378, LOC644554
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057428
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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